Myong Subin, Cosby Jenna K, Padilla Brianna N, Opozda David M, Kahn Jacob D, Akter Naima, O Apos Toole Eileen T, Nannas Natalie J
Department of Biology, Hamilton College, Clinton, New York, USA.
Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado, USA.
Cytogenet Genome Res. 2025 Jul 29:1-17. doi: 10.1159/000547002.
Spindles are microtubules-based machines whose primary function is to accurately segregate chromosomes in both mitotic and meiotic cell division. The structure of spindles is critical for their function; errors in morphology or attachment to chromosomes lead to aneuploidy, potentially resulting in disease, infertility, and lethality. Electron microscopy studies have yielded fine-detail spindle ultrastructures in many plant and animal species, but no studies have investigated the spindle of Zea mays, a critical crop, and cytogenetic model system.
Here we use electron tomography (ET), reconstruction, and modeling to obtain three-dimensional, nanometer-resolution of the Z. mays meiotic spindle. Structures such as microtubules, kinetochores, vesicles, membrane channels, and nuclear envelope were modeled through a partial spindle reconstruction, and confirmed using immunostaining and live fluorescence microscopy.
ET revealed that maize spindles contain 8-18 kinetochore microtubules (kMTs) per kinetochore, which are approximately 776 nm in diameter and 316 nm in depth. Small ∼37 nm vesicles were identified, as well as larger (∼5 µm long, 800 nm wide) membrane structures with channels that allow spindle microtubules to pass through. These membrane channels stain positively for the ER-marker protein disulfide isomerase. Imaging of prophase meiotic cells revealed a cross-hatch microtubule arrangement in the perinuclear ring on the external surface of the nuclear envelope, which also contained type II nuclear grooves with transnuclear microtubules passing from the nucleus to the cytoplasm.
Z. mays meiotic spindles are similar to animal counterparts with a comparable number of kMTs and pre-spindle transnuclear microtubules but also plant-specific features such as Golgi-derived vesicles to assist cell plate formation, internal ER membrane channels, and a perinuclear microtubule ring that aids spindle assembly. Maize kinetochores have an electron-diffuse ball in cup morphology that is comparable in size to Drosophila kinetochores and larger than mammalian kinetochores.
纺锤体是以微管为基础的细胞器,其主要功能是在有丝分裂和减数分裂细胞分裂过程中准确地分离染色体。纺锤体的结构对其功能至关重要;形态或与染色体附着方面的错误会导致非整倍体,可能引发疾病、不孕和致死。电子显微镜研究已在许多动植物物种中揭示了纺锤体精细的超微结构,但尚未有研究对重要作物和细胞遗传学模型系统玉米的纺锤体进行探究。
在此,我们使用电子断层扫描(ET)、重建和建模来获得玉米减数分裂纺锤体的三维纳米分辨率图像。通过部分纺锤体重建对微管、动粒、囊泡、膜通道和核膜等结构进行建模,并使用免疫染色和活细胞荧光显微镜进行确认。
ET显示,玉米纺锤体每个动粒含有8 - 18条动粒微管(kMTs),其直径约为776纳米,深度约为316纳米。识别出了直径约37纳米的小囊泡,以及更大的(约5微米长,800纳米宽)带有允许纺锤体微管穿过的通道的膜结构。这些膜通道对内质网标记蛋白二硫键异构酶呈阳性染色。减数分裂前期细胞成像显示,在核膜外表面的核周环中有交叉网状微管排列,其中还包含II型核沟,有跨核微管从细胞核通向细胞质。
玉米减数分裂纺锤体与动物的类似,具有相当数量的kMTs和纺锤体前跨核微管,但也具有植物特有的特征,如有助于细胞板形成的高尔基体衍生囊泡、内部内质网膜通道以及辅助纺锤体组装的核周微管环。玉米动粒具有杯状电子弥散球形态,其大小与果蝇动粒相当,大于哺乳动物动粒。